Variant DetailsVariant: esv3613764Internal ID | 6653972 | Landmark | | Location Information | | Cytoband | 7q11.23 | Allele length | Assembly | Allele length | hg38 | 15245 | hg19 | 15245 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12848890, essv12848885, essv12848888, essv12848886, essv12848891, essv12848887, essv12848889 | Samples | NA19701, HG02860, NA19681, NA20753, NA21098, NA20851, NA21123 | Known Genes | DTX2, UPK3B | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3613764
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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